KR900000405A - Polysilazane, its production method and its use as ceramic precursor, and said ceramics - Google Patents

Polysilazane, its production method and its use as ceramic precursor, and said ceramics Download PDF

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KR900000405A
KR900000405A KR1019890008593A KR890008593A KR900000405A KR 900000405 A KR900000405 A KR 900000405A KR 1019890008593 A KR1019890008593 A KR 1019890008593A KR 890008593 A KR890008593 A KR 890008593A KR 900000405 A KR900000405 A KR 900000405A
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hydrazine
sicl
silicon
polysilazane
atoms
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KR1019890008593A
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Korean (ko)
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크리스띠앙 꼴롱비에
쟝-삐에르 뀌에
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미셸 로셰
소시에떼 아토샹
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/48Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
    • C08G77/54Nitrogen-containing linkages
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G77/00Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
    • C08G77/60Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which all the silicon atoms are connected by linkages other than oxygen atoms
    • C08G77/62Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/56Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides
    • C04B35/565Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide
    • C04B35/571Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on carbides or oxycarbides based on silicon carbide obtained from Si-containing polymer precursors or organosilicon monomers
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B35/00Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/515Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics
    • C04B35/58Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides
    • C04B35/584Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicon nitride
    • C04B35/589Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on non-oxide ceramics based on borides, nitrides, i.e. nitrides, oxynitrides, carbonitrides or oxycarbonitrides or silicides based on silicon nitride obtained from Si-containing polymer precursors or organosilicon monomers

Abstract

내용 없음No content

Description

폴리실라잔, 그의 제조방법 및 그의 세라믹 전구체로서의 용도, 및 상기 세라믹Polysilazane, its production method and its use as ceramic precursor, and said ceramics

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (12)

적어도 하나의 규소원자가 및 적어도 하나의 질소원자가 단위 사이의 결합을 제공하여 직쇄, 측쇄 또는 고리형 쇄의 배열을 형성하는 하기식(Ⅰ)의 단위로 구성되며.Wherein at least one silicon atom and at least one nitrogen atom provide a bond between units to form an array of straight, branched or cyclic chains. 규소유효 원자가의 적어도 일부는 수소원자 및/ 또는 불포화 지방족 탄화수소기에 결합되고, 규소 및 질소의 남은 원자가는 수소원자, 탄소수 18이하의 불포화 지방족 탄화수소기 또는 알킬, 시클로알킬, 모노-또는 폴리시클릭아릴, 알킬아릴 또는 아릴알킬기에 결합될 수 있음을 특징으로 하는 폴리실라잔.At least a portion of the silicon effective valency is bonded to a hydrogen atom and / or an unsaturated aliphatic hydrocarbon group, and the remaining valences of silicon and nitrogen are hydrogen atoms, unsaturated aliphatic hydrocarbon groups having up to 18 carbon atoms or alkyl, cycloalkyl, mono- or polycyclicaryl, Polysilazane, which may be bonded to an alkylaryl or arylalkyl group. 제1항에 있어서, 분자량이 200 내지 50,000사이, 바람직하게는 400 내지 10,000사이임을 특징으로 하는 폴리실라잔.2. Polysilazane according to claim 1, characterized in that the molecular weight is between 200 and 50,000, preferably between 400 and 10,000. 제1항 또는 2항에 있어서, 규소 및 질소원자의 치환제가 수소나 불포화 지방족 탄화수소기를 나타내지 않을 경우, 그 치환체가 탄소수 1~8의 포화 지방족 탄화수소, 탄소수 3~7의 지방족 고리기 및 페닐, 벤질, 페닐에틸, 톨릴, 크실릴 또는 나프틸기로 이루어지는 군에서 선택됨을 특징으로 하는 폴리실라잔.The substituent according to claim 1 or 2, wherein when the substituents of silicon and nitrogen atoms do not represent hydrogen or unsaturated aliphatic hydrocarbon groups, the substituents are saturated aliphatic hydrocarbons of 1 to 8 carbon atoms, aliphatic ring groups of 3 to 7 carbon atoms, and phenyl and benzyl , Phenylethyl, tolyl, xylyl or naphthyl group. 하기식(Ⅱ)의 할로실란 1종 이상을 하기식(Ⅲ)의 히드라진 1종 이상과 반응시키는 것으로 구성됨을 특징으로 하는 제1 내지 3항중 어느 한항에 따르는 폴리실라잔의 제조방법.A method for producing polysilazane according to any one of claims 1 to 3, wherein the halosilane of formula (II) is reacted with at least one hydrazine of formula (III). [식중, Y는 할로겐원자, 특히 염소를 나타내고, a는 1 이상 4이하의 정수, 바람직하게는 약 2이며, 규소 및 질소의 자유원자가(들)은 수소원자, 불포화 지방족 탄화수소기 또는 식(Ⅰ)의 범위에서 언급된 기타 작용기중의 하나와 결합되어 있다.][Wherein Y represents a halogen atom, in particular chlorine, a is an integer of 1 or more and 4 or less, preferably about 2, and the free atom (s) of silicon and nitrogen are a hydrogen atom, an unsaturated aliphatic hydrocarbon group or Combined with one of the other functional groups mentioned in the scope of 제4항에 있어서, 할로실란이 하기식의 화합물로 이루어지는 군에서 선택됨을 특징으로 하는 방법.The method of claim 4, wherein the halosilane is selected from the group consisting of compounds of the formula: SiCl4, (CH3)2SiCl2, (CH3)3SiClSiCl 4 , (CH 3 ) 2 SiCl 2 , (CH 3 ) 3 SiCl CH3SiCl3, (C6H5)2SiCl2, (C6H5)(CH3)SiCl2 CH 3 SiCl 3 , (C 6 H 5 ) 2 SiCl 2 , (C 6 H 5 ) (CH 3 ) SiCl 2 (C6H5)SiCl3, (CH3)(CH3CH2)SiCl2 (C 6 H 5 ) SiCl 3 , (CH 3 ) (CH 3 CH 2 ) SiCl 2 H2SiCl2, (CH3)2HSiCl, HSiCl3 H 2 SiCl 2 , (CH 3 ) 2 HSiCl, HSiCl 3 CH3(CH2=CH)SiCl2, (CH3)2(CH2=CH)SiClCH 3 (CH 2 = CH) SiCl 2 , (CH 3 ) 2 (CH 2 = CH) SiCl (CH3)HSiCl2 (CH 3 ) HSiCl 2 제4항 또는 5항에 있어서, 히드라진이 비치환 히드라진(N2H4), 메틸히드라진, 에틸히드라진, 페닐히드라진, 시클로헥실히드라진, 디메틸히드라진, 디에틸히드라진, 디페닐히드라진, 디벤질히드라진, α-나프틸히드라진, 디이소프로필히드라진, 디톨릴히드라진, 디이소부틸히드라진, (디메틸페닐)히드라진 및 디(α-나프틸)히드라진으로 이루어진 군에서 선택됨을 특징으로 하는 방법.The hydrazine according to claim 4 or 5, wherein the hydrazine is an unsubstituted hydrazine (N 2 H 4 ), methyl hydrazine, ethyl hydrazine, phenyl hydrazine, cyclohexyl hydrazine, dimethyl hydrazine, diethyl hydrazine, diphenyl hydrazine, dibenzyl hydrazine, α -Naphthylhydrazine, diisopropylhydrazine, ditolylhydrazine, diisobutylhydrazine, (dimethylphenyl) hydrazine and di (α-naphthyl) hydrazine. 제4 내지 6항중 어느 한 항에 있어서, 규소원자의 몰수에 첨가된 할로겐원자 Y의 몰수보다 히드라진의 몰수가 크도록 히드라진의 양을 사용함을 특징으로 하는 방법.The method according to any one of claims 4 to 6, wherein the amount of hydrazine is used so that the number of moles of hydrazine is greater than the number of moles of halogen atoms Y added to the number of moles of silicon atoms. 제4 내지 7항중 어느 한 항에 있어서, 반응이 3차 아민의 존재하에 수행됨을 특징으로 하는 방법.8. Process according to any of claims 4 to 7, characterized in that the reaction is carried out in the presence of a tertiary amine. 제8항에 있어서, 히드라진의 몰수가 규소원자의 몰수보다 큰 것을 특징으로 하는 방법.9. The method of claim 8, wherein the number of moles of hydrazine is greater than that of silicon atoms. 제8항 또는 9항에 있어서, 3차 아민이 트리에틸아민, 트리메틸아민, 트리페닐아민 및 피리딘으로 이루어지는 군에서 선택됨을 특징으로 하는 방법.10. The process according to claim 8 or 9, wherein the tertiary amine is selected from the group consisting of triethylamine, trimethylamine, triphenylamine and pyridine. 섬유, 필라멘트, 분말, 필름, 장식면(facing), 플레이크, 도관, 기포체 또는 직물이나 부직물 또는 이들의 복합재료와 같은 성형품의 형태인 것을 특징으로 하는 제1항 내지 제3항중 어느 한항에 따르는 폴리실라잔.The method according to any one of claims 1 to 3, characterized in that it is in the form of fibers, filaments, powders, films, facings, flakes, conduits, foams or shaped articles such as woven or nonwovens or composites thereof. Pouring polysilazane. 하기 비율(중량%)의 원소를 함유하고 : -30~70%의 Si, -2~30%의 N, -0~35%의 C, -0~25%의 O : 제11항에 따르는 성형된 폴리실라잔을 열분해함으로써 수득되는 것을 특징으로 하는 세라믹 제품.Molding according to claim 11, containing elements in the following proportions (wt%): -30 to 70% Si, -2 to 30% N, -0 to 35% C, -0 to 25% O Ceramic product, which is obtained by pyrolysing polysilazane. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019890008593A 1988-06-22 1989-06-21 Polysilazane, its production method and its use as ceramic precursor, and said ceramics KR900000405A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR8808384 1988-06-22
FR8808384A FR2633301A1 (en) 1988-06-22 1988-06-22 POLYSILAZANES, PROCESS FOR PREPARING THEM, THEIR USE AS PRECURSORS OF CERAMICS AND CERAMIC DISHES

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JP (1) JPH0251530A (en)
KR (1) KR900000405A (en)
CN (1) CN1038655A (en)
AU (1) AU3665289A (en)
DK (1) DK306789A (en)
FR (1) FR2633301A1 (en)
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FR2635528A1 (en) * 1988-08-17 1990-02-23 Atochem PROCESS FOR THE PREPARATION OF POLYHYDROSILAZANES DERIVED FROM HYDRAZINE AND THE USE OF SAID SILAZANES AS CERAMIC PRECURSORS
FR2653131A1 (en) * 1989-10-17 1991-04-19 Rhone Poulenc Chimie PROCESS FOR THE PREPARATION OF POLYORGANOSILAZANE OF HIGH MOLECULAR WEIGHT
FR2693204A1 (en) * 1992-08-27 1994-01-07 Atochem Elf Sa Poly:silyl-hydrazine(s) prepn., used as coatings on e.g. ceramics, metals or metalloid(s) - comprises reacting halo-silane(s) or di:silane(s) with hydrazine(s) in presence of inert solvent
US7122222B2 (en) 2003-01-23 2006-10-17 Air Products And Chemicals, Inc. Precursors for depositing silicon containing films and processes thereof
JP5813006B2 (en) * 2009-12-22 2015-11-17 スリーエム イノベイティブ プロパティズ カンパニー Process for preparing storage stable curable polysilazane and polysilazane prepared thereby

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DE2218960A1 (en) * 1972-04-19 1973-11-08 Bayer Ag MOLDED BODIES FROM MOGENIC MIXTURES OF SILICON CARBIDE AND SILICON NITRIDE AND PROCESS FOR THEIR PRODUCTION
US4612383A (en) * 1985-04-26 1986-09-16 S R I International Method of producing polysilazanes
FR2577933B1 (en) * 1985-02-27 1987-02-20 Rhone Poulenc Rech PROCESS FOR THE PREPARATION OF ORGANOPOLYSILAZANES AND ORGANOPOLY (DISILYL) SILAZANES WITH IMPROVED THERMAL RESISTANCE AND THE USE THEREOF IN PARTICULAR AS A CERAMIC PRECURSOR
FR2590584B1 (en) * 1985-11-28 1988-03-04 Rhone Poulenc Spec Chim PROCESS FOR THE PREPARATION, IN TWO STEPS, OF CROSS-LINKS OF ORGANOPOLYSILAZANES WITH IMPROVED THERMAL RESISTANCE, WHICH MAY BE USED IN PARTICULAR AS A CERAMIC PRECURSOR
FR2590580B1 (en) * 1985-11-28 1988-05-13 Rhone Poulenc Spec Chim PROCESS FOR THE CATALYTIC TREATMENT OF A POLYSILAZANE COMPRISING AT LEAST TWO HYDROCARBON GROUPS WITH ALIPHATIC unsATURATION BY MOLECULE
CA1302619C (en) * 1987-06-08 1992-06-02 Gary Thomas Burns Silane modified polysilacyclobutasilazanes
JP2750406B2 (en) * 1988-02-08 1998-05-13 東燃株式会社 Modified polysilazane and method for producing the same

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DK306789D0 (en) 1989-06-21
NO892570L (en) 1989-12-27
CN1038655A (en) 1990-01-10
AU3665289A (en) 1990-01-04
JPH0251530A (en) 1990-02-21
EP0351262A1 (en) 1990-01-17
DK306789A (en) 1989-12-23
NO892570D0 (en) 1989-06-21

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